Canonical Allele Identifier: CA402939158

Gene: GPX4

Linked Data

• dbSNP Id: rs1249650926
• gnomAD v4: 19-1106251-G-A
• MyVariant Identifiers: chr19:g.1106250G>A (hg19) ; chr19:g.1106251G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106251G>A , CM000681.2:g.1106251G>A	GRCh38
NC_000019.9:g.1106250G>A , CM000681.1:g.1106250G>A	GRCh37
NC_000019.8:g.1057250G>A	NCBI36
NG_050621.1:g.7326G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.597G>A	ENSP00000473614.3:p.Lys199=
ENST00000593032.6:c.466G>A	ENSP00000465828.4:p.Val156Met
ENST00000706713.1:c.480G>A	ENSP00000516510.1:p.Lys160=
ENST00000706714.1:c.466G>A	ENSP00000516511.1:p.Val156Met
ENST00000706715.1:c.102G>A	ENSP00000516512.1:p.Lys34=
ENST00000354171.13:c.486G>A MANE Select	ENSP00000346103.7:p.Lys162=
ENST00000589115.6:c.477-149G>A	ENSP00000466872.3:n.477-149G>A
ENST00000354171.12:c.486G>A	ENSP00000346103.7:p.Lys162=
ENST00000585480.1:c.219G>A	ENSP00000467900.1:p.Lys73=
ENST00000587648.5:c.366G>A	ENSP00000468349.1:p.Lys122=
ENST00000588919.5:c.405G>A	ENSP00000464989.3:p.Lys135=
ENST00000589115.5:c.477-149G>A	ENSP00000466872.2:n.477-149G>A
ENST00000592940.2:n.857G>A
ENST00000593032.5:c.466G>A	ENSP00000465828.3:p.Val156Met
ENST00000611653.4:c.405G>A	ENSP00000483655.1:p.Lys135=
ENST00000616066.4:c.483G>A	ENSP00000485000.1:p.Lys161=
ENST00000622390.4:c.594G>A	ENSP00000477503.1:p.Lys198=
NM_001039847.2:c.486G>A	NP_001034936.1:p.Lys162=
NM_001039848.2:c.597G>A	NP_001034937.1:p.Lys199=
NM_002085.4:c.486G>A	NP_002076.2:p.Lys162=
NM_001039848.3:c.597G>A	NP_001034937.1:p.Lys199=
NM_001039847.3:c.486G>A	NP_001034936.1:p.Lys162=
NM_001039848.4:c.597G>A	NP_001034937.1:p.Lys199=
NM_001367832.1:c.405G>A	NP_001354761.1:p.Lys135=
NM_002085.5:c.486G>A MANE Select	NP_002076.2:p.Lys162=